A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520654



Internal ID21845013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:232581434..232581434hg38UCSC Ensembl
chr2:233446144..233446144hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054336
Supporting Variants
Samples
Known GenesEIF4E2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520654
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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